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Review
. 2022 Dec 12:13:1063413.
doi: 10.3389/fphar.2022.1063413. eCollection 2022.

Transporter and metabolizer gene polymorphisms affect fluoroquinolone pharmacokinetic parameters

Affiliations
Review

Transporter and metabolizer gene polymorphisms affect fluoroquinolone pharmacokinetic parameters

Nurul Annisa et al. Front Pharmacol. .

Abstract

Tuberculosis (TB) is an infectious disease that occurs globally. Treatment of TB has been hindered by problems with multidrug-resistant strains (MDR-TB). Fluoroquinolones are one of the main drugs used for the treatment of MDR-TB. The success of therapy can be influenced by genetic factors and their impact on pharmacokinetic parameters. This review was conducted by searching the PubMed database with keywords polymorphism and fluoroquinolones. The presence of gene polymorphisms, including UGT1A1, UGT1A9, SLCO1B1, and ABCB1, can affect fluoroquinolones pharmacokinetic parameters such as area under the curve (AUC), creatinine clearance (CCr), maximum plasma concentration (Cmax), half-life (t1/2) and peak time (tmax) of fluoroquinolones.

Keywords: ABCB1; SLCO1B1; UGT1A1; UGT1A9; moxifloxacin; pharmacogenetics; sitafloxacin; trovafloxacin.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

FIGURE 1
FIGURE 1
Fluoroquinolones pharmacokinetic parameter affected by gene polymorphisms.

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